GMP Audit Check List- Storage of Starting Materials

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GMP Audit Check List- Storage of Starting Materials

🏭 GMP Audit Checklist – Storage of Starting Materials

1. Material Receipt & Identification

  • ✅ Are incoming starting materials received against approved suppliers and purchase orders?

  • ✅ Are materials inspected for damage, tampering, contamination, and labeling before acceptance?

  • ✅ Are quarantine materials physically or electronically segregated?

  • ✅ Are materials labeled with unique IDs, batch/lot numbers, and status (Quarantine/Released/Rejected)?

  • ✅ Is sampling done in a controlled area by trained personnel as per SOP?


2. Storage Conditions & Controls

  • ✅ Are materials stored under recommended temperature and humidity conditions?

  • ✅ Are temperature/humidity monitoring devices installed, calibrated, and records maintained?

  • ✅ Are mapping studies performed for warehouses, cold rooms, and freezers?

  • ✅ Is there an alarm system for excursions with documented corrective actions?

  • ✅ Are materials stored off the floor (on pallets/racks) and away from walls for cleaning & inspection access?


3. Segregation & Labeling

  • ✅ Are rejected, expired, or returned materials segregated in a controlled area?

  • ✅ Are hazardous, flammable, or light-sensitive materials stored as per safety guidelines?

  • ✅ Is there clear status labeling (“Quarantine,” “Released,” “Rejected”) for all containers?

  • ✅ Is FEFO/FIFO (First Expired/First Out or First In/First Out) system implemented?


4. Documentation & Traceability

  • ✅ Are warehouse logbooks and material movement records complete and contemporaneous?

  • ✅ Are electronic systems (ERP/SAP) validated and access-controlled?

  • ✅ Are inventory levels regularly reconciled with records?

  • ✅ Are deviations in material handling (spillage, mix-up, temperature excursion) documented and investigated?


5. Sampling & Dispensing Areas

  • ✅ Are sampling and dispensing areas controlled (dust extraction, gowning, cross-contamination prevention)?

  • ✅ Are balances calibrated before use in dispensing?

  • ✅ Is line clearance performed before each operation?

  • ✅ Are materials weighed/dispensed under proper labeling to avoid mix-ups?


6. Housekeeping & Safety

  • ✅ Are storage areas clean, pest-free, and free from unnecessary items?

  • ✅ Are pest control records up to date?

  • ✅ Are fire extinguishers, alarms, and safety signs available?

  • ✅ Is PPE used appropriately when handling hazardous materials?


7. Periodic Review & Compliance

  • ✅ Are materials periodically reviewed for shelf-life and retesting needs?

  • ✅ Are expired/rejected materials immediately labeled and stored in a separate controlled area?

  • ✅ Is there a system for disposal/destruction of obsolete materials?

  • ✅ Are GMP training records of warehouse staff current?


📌 Quick Pre-Audit Focus Points

  • Material status labeling & segregation

  • Temperature & humidity monitoring compliance

  • Documentation completeness & traceability

  • Expired/rejected materials control

  • Sampling & dispensing hygiene

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